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呼吸道病变中6型人乳头瘤病毒亚型mRNA的异质性。

Heterogeneity in mRNA of human papillomavirus type-6 subtypes in respiratory tract lesions.

作者信息

Ward P, Mounts P

机构信息

Department of Immunology and Infectious Diseases, Johns Hopkins University School of Public Health, Baltimore, Maryland 21205.

出版信息

Virology. 1989 Jan;168(1):1-12. doi: 10.1016/0042-6822(89)90397-8.

Abstract

We have analyzed the structure of viral transcripts in six HPV-6c-induced respiratory tract lesions, which included four benign laryngeal papilloma, one benign nasopapilloma, and one malignant tumor, in four benign laryngeal papilloma induced by HPV-6e, and in one benign laryngeal papilloma induced by HPV-6f. Northern analysis and S1 nuclease digestion with subgenomic RNA probes demonstrated that the major exon of 1050 bases had a 5' end in the E4 open reading frame and a 3' end in E5B. Primer extension from a synthetic oligonucleotide in E4 was used to examine sequences 5' to the major exon. Differences were found in length, start sites, and relative abundance of the first exon in transcripts produced in HPV-6c-induced infections as compared to HPV-6e- and HPV-6f-induced infections. Primer extension in the presence of dideoxynucleotides facilitated sequence analyses of the first exon. HPV-6c transcripts contained common sequences from E1 that in different transcripts extended farther upstream in the 5' direction into E7 resulting in different lengths. All of the mRNAs had the same splice junction at nucleotide 847 in E1 and 3325 in E4. Similarly, the HPV-6e transcripts shared common sequences in the first exon that differed in length as a result of different starting points and had the same splice junction as the HPV-6c transcripts. No differences were found in the structure of viral transcripts in a malignant vs benign lesions, nor in those of nasopapilloma vs laryngeal papilloma when induced by the same HPV-6 subtype.

摘要

我们分析了6例HPV - 6c诱发的呼吸道病变、4例HPV - 6e诱发的良性喉乳头瘤以及1例HPV - 6f诱发的良性喉乳头瘤中病毒转录本的结构,其中6例HPV - 6c诱发的呼吸道病变包括4例良性喉乳头瘤、1例良性鼻乳头瘤和1例恶性肿瘤。用亚基因组RNA探针进行的Northern分析和S1核酸酶消化表明,1050个碱基的主要外显子5'端位于E4开放阅读框,3'端位于E5B。用E4中的合成寡核苷酸进行引物延伸,以检测主要外显子5'端的序列。与HPV - 6e和HPV - 6f诱发的感染相比,发现HPV - 6c诱发的感染所产生的转录本中,第一个外显子的长度、起始位点和相对丰度存在差异。在双脱氧核苷酸存在的情况下进行引物延伸,有助于对第一个外显子进行序列分析。HPV - 6c转录本包含来自E1的共同序列,这些序列在不同的转录本中在5'方向上进一步向上游延伸至E7,导致长度不同。所有mRNA在E1的核苷酸847和E4的3325处具有相同的剪接连接。同样,HPV - 6e转录本在第一个外显子中共享共同序列,由于起始点不同,其长度也不同,并且与HPV - 6c转录本具有相同的剪接连接。在恶性病变与良性病变中,以及在由相同HPV - 6亚型诱发的鼻乳头瘤与喉乳头瘤中,未发现病毒转录本结构存在差异。

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